NDC 41520-909 Complete Beauty
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Co
- 41520-909 - Complete Beauty
Product Packages
NDC Code 41520-909-26
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE / 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 41520-909?
What are the uses for Complete Beauty?
Which are Complete Beauty UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Complete Beauty Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- LAURETH-7 (UNII: Z95S6G8201)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
- DOCOSANOL (UNII: 9G1OE216XY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- STEARETH-2 (UNII: V56DFE46J5)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PANTHENOL (UNII: WV9CM0O67Z)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".